BaseSpace
Correlation
Engine-Public
Sign In
Register
Correlation Engine 2.0
Home
My Data
Bookmarks
Collaborations
Inbox
Import Your Data
QuickView
FAQ
What is QuickView?
What can my QuickView results tell me?
What are the sources for the General Info tab in QuickView?
More QuickView FAQs
Back to top
QuickView
Curated
Studies
Body
Atlas
Disease
Atlas
Pharmaco
Atlas
Knockdown
Atlas
Genetic
Markers
Pathway
Enrichment
Literature
Clinical
Trials
0
Meta-
Analysis
QuickView
Search sequence regions
(e.g.
SLC12A1
,
nitric oxide metabolic process
,
Inflammatory disorder
,
Lymphocyte
)
Organisms
Chromosomes
Start
Stop
Homo Sapiens
Mus Musculus
Rattus Norvegicus
C. Elegans
D. Melanogaster
Saccharomyces Cerevisiae
QuickView
Go back to main search
Bookmark
Forward
QuickView
for
Weill-Marchesani syndrome
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
ADAMTS10
FBN1
No SNPs found
Explore Genetic Markers Results
Pathway Enrichment
Most Correlated Biogroups
microfibril
extracellular matrix
GRAESSMANN_APOPTOSIS_BY_SERUM_DEPRIVATION_UP
Fibrillin
sequestering of TGFbeta in extracellular matrix
Explore Pathway Enrichment Results
Curated Studies
Most Correlated Studies
OMIM - Congenital disorder
Explore Curated Studies Results
Literature
Most Relevant Literature
LTBP2 mutations cause Weill-Marchesani and Weill-Marchesani-like syndrome and affect disruptions in …
Familial spherophakia with short stature caused by a novel homozygous ADAMTS17 mutation.
Microenvironmental regulation by fibrillin-1.
An ADAMTS17 splice donor site mutation in dogs with primary lens luxation.
Clinical and genetic investigation of isolated microspherophakia in a consanguineous Tunisian family…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Thoracic Aortic Dilatation Syndromes
Safety and Performance Study of the ARGOS-IO (Intraocular) System in Patients With Primary Open Angl…
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ